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Non-invasive prenatal testing using massively parallel sequencing of maternal plasma DNA: From molecular karyotyping to fetal whole-genome sequencing

机译:使用母体血浆DNA的大规模平行测序进行的非侵入性产前检查:从分子核型分析到胎儿全基因组测序

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The discovery of cell-free fetal DNA in maternal plasma in 1997 has stimulated a rapid development of non-invasive prenatal testing. The recent advent of massively parallel sequencing has allowed the analysis of circulating cell-free fetal DNA to be performed with unprecedented sensitivity and precision. Fetal trisomies 21, 18 and 13 are now robustly detectable in maternal plasma and such analyses have been available clinically since 2011. Fetal genome-wide molecular karyotyping and whole-genome sequencing have now been demonstrated in a number of proof-of-concept studies. Genome-wide and targeted sequencing of maternal plasma has been shown to allow the non-invasive prenatal testing of β-thalassaemia and can potentially be generalized to other monogenic diseases. It is thus expected that plasma DNA-based non-invasive prenatal testing will play an increasingly important role in future obstetric care. It is thus timely and important that the ethical, social and legal issues of non-invasive prenatal testing be discussed actively by all parties involved in prenatal care. The discovery of cell-free fetal DNA in maternal plasma in 1997 has stimulated a rapid development of non-invasive prenatal testing. The recent advent of high-throughput sequencing technologies has allowed the analysis of circulating cell-free fetal DNA to be performed with unprecedented sensitivity and precision. A number of fetal chromosomal disorders are now robustly detectable in maternal plasma and such analyses have been available clinically since 2011. Moving beyond selected fetal chromosomal disorders, fetal single-gene disorders and even fetal whole-genome analysis have now been demonstrated in a number of proof-of-concept studies. It is thus expected that DNA-based non-invasive prenatal testing will play an increasingly important role in future obstetrics care. It is thus timely and important that the ethical, social and legal issues of non-invasive prenatal testing be actively discussed by all parties involved in prenatal care.
机译:1997年孕妇血浆中无细胞胎儿DNA的发现刺激了非侵入性产前检测的迅速发展。大规模并行测序的最新出现使得循环无细胞胎儿DNA的分析能够以前所未有的灵敏度和精确度进行。胎儿三体性21、18和13现在可以在母体血浆中可靠地检测到,并且这种分析自2011年以来就已经在临床上可用。胎儿的全基因组分子核型分析和全基因组测序现已在许多概念验证研究中得到证明。研究表明,对母体血浆进行全基因组靶向测序可以对β地中海贫血进行无创的产前检测,并有可能推广至其他单基因疾病。因此,预期基于血浆DNA的非侵入性产前检查将在未来的产科护理中发挥越来越重要的作用。因此,及时和重要的是,与产前保健有关的所有各方应积极讨论无创产前检查的道德,社会和法律问题。 1997年,孕妇血浆中无细胞胎儿DNA的发现刺激了非侵入性产前检测的迅速发展。最近,高通量测序技术的出现使循环无细胞胎儿DNA的分析能够以前所未有的灵敏度和精度进行。现在可以从母体血浆中可靠地检测出许多胎儿染色体疾病,并且这种分析自2011年以来已在临床上可用。除了某些胎儿染色体疾病之外,在许多研究中还证明了胎儿单基因疾病甚至是胎儿全基因组分析。概念验证研究。因此,预期基于DNA的非侵入性产前检查将在未来的产科护理中发挥越来越重要的作用。因此,及时和重要的是,参与产前检查的所有各方应积极讨论无创产前检查的道德,社会和法律问题。

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